WNT10A - Gene browser | 3billion

WNT10A

WNT10A

Wnt family member 10A

HCNC Approved Symbol: WNT10A (HGNC:13829)
Genomic Coordinates: 2:218,874,116 - 218,893,928 (2q35)
Synonyms
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the WNT10A gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

02
Patient count

Dental agenesis: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Ectodermal dysplasia, anhidrotic: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

WNT10A - Gene browser | 3billion